Nuvasive, Inc.
NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW
SKU K001323UPC MRW
In Stock
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FDA 510(k) Cleared (K001323)
1
Free shipping on orders over $99 · 30-day returns
Nuvasive, Inc.
Free shipping on orders over $99 · 30-day returns
NUVASIVE PERCUTANEOUS TRANSFACET/INTRAPEDICULAR SCREW is an FDA 510(k)-cleared medical device (K001323) manufactured by Nuvasive, Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on July 24, 2000.
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